Pro-Dex Inc recalls Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical s…
- Recall date
- December 23, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1095-2016
- FDA classification
- Class II
- Brand / firm
- Pro-Dex Inc
- Sold / distributed
- Distributed in FL.
Why it was recalled
The sterile battery may contain particulates within the sterile package.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).
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